EP2370547A1 - Anhydride demulsifier formulations for resolving emulsions of water and oil - Google Patents
Anhydride demulsifier formulations for resolving emulsions of water and oilInfo
- Publication number
- EP2370547A1 EP2370547A1 EP09792457A EP09792457A EP2370547A1 EP 2370547 A1 EP2370547 A1 EP 2370547A1 EP 09792457 A EP09792457 A EP 09792457A EP 09792457 A EP09792457 A EP 09792457A EP 2370547 A1 EP2370547 A1 EP 2370547A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- oil
- water
- demulsifier
- anhydride
- composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 117
- 239000000839 emulsion Substances 0.000 title claims abstract description 76
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 76
- 150000008064 anhydrides Chemical class 0.000 title claims abstract description 52
- 238000009472 formulation Methods 0.000 title description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims abstract description 100
- 239000003921 oil Substances 0.000 claims abstract description 56
- 239000010779 crude oil Substances 0.000 claims abstract description 34
- -1 aryl anhydrides Chemical class 0.000 claims abstract description 18
- 238000000034 method Methods 0.000 claims description 30
- 239000002904 solvent Substances 0.000 claims description 19
- 230000008569 process Effects 0.000 claims description 17
- 239000012530 fluid Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 238000010796 Steam-assisted gravity drainage Methods 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 229920000151 polyglycol Polymers 0.000 claims description 6
- 239000010695 polyglycol Substances 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 5
- 150000007513 acids Chemical class 0.000 claims description 5
- 229920005862 polyol Polymers 0.000 claims description 5
- 150000003077 polyols Chemical class 0.000 claims description 5
- 229920001568 phenolic resin Polymers 0.000 claims description 4
- 229920000768 polyamine Polymers 0.000 claims description 4
- 150000002170 ethers Chemical class 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- 239000005011 phenolic resin Substances 0.000 claims description 3
- 239000010426 asphalt Substances 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 239000000446 fuel Substances 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- 238000011282 treatment Methods 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 238000007670 refining Methods 0.000 description 7
- 238000012360 testing method Methods 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 5
- 230000008014 freezing Effects 0.000 description 5
- 238000007710 freezing Methods 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000007762 w/o emulsion Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- 229930185605 Bisphenol Natural products 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000012993 chemical processing Methods 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 238000011033 desalting Methods 0.000 description 2
- 238000009882 destearinating Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000002563 ionic surfactant Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 150000004075 acetic anhydrides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002332 oil field water Substances 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 238000012261 overproduction Methods 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/02—Separation of non-miscible liquids
- B01D17/04—Breaking emulsions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/02—Separation of non-miscible liquids
- B01D17/04—Breaking emulsions
- B01D17/047—Breaking emulsions with separation aids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G33/00—Dewatering or demulsification of hydrocarbon oils
- C10G33/04—Dewatering or demulsification of hydrocarbon oils with chemical means
Definitions
- This invention relates to demulsifier compositions and methods. for resolving emulsions of water and oil. More particularly, the invention relates to resolving water external emulsions of water and oil and complex emulsions of water and oil. The invention also relates to anhydride compositions including one or more anhydrides for use as a demulsifier or as a component in demulsifier compositions for use in resolving such emulsions of water and oil.
- This invention has particular applicability in cold climates where low temperature stability is required.
- Crude oil produced from geological formations can contain various amounts of water.
- Water and crude oil are naturally non-miscible; however, when naturally occurring interfacial active compounds are present, these compounds can aggregate on the water and oil interface and cause water to form droplets within the bulk oil phase.
- interfacial active compounds When crude oil lifting through production tubings, the water and oil encounters an increased mixing energy from rapid flow through chokes and bends. This additional mixing energy can emulsify the water and oil.
- Such an oil external, water internal two -phase system is commonly referred to as a crude oil emulsion, which can be quite stable.
- the presence of water in crude oil can interfere with refining operations, induce corrosion, increase heat capacity, and result in reduced handling capacity of pipelines and refining equipment.
- the crude oil that is to be shipped out of the oilfield should be practically free of water and usually has a maximum water content limit of about 0.5 to 3% by total weight, depending on the type of crude and oil company.
- the emulsified water can also contain various amounts of salts. These salts are detrimental to crude oil refrning processes due to potential corrosion in the refinery.
- desalting techniques comprise the deliberate mixing of the incoming crude oil with a fresh "wash water” to extract the water soluble salts and hydrophilic solids from the crude oil.
- emulsion-breaking chemicals or demulsifiers include alkylphenol formaldehyde resin alkoxylates (AFRA), polyalkylene glycols (PAG), organic sulfonates, and the like. These compounds, however, may not provide satisfactory performance in all instances. In particular, in extremely cold weather (e.g., -40 0 C and below) various problems are known. These active ingredients are typically viscous and require a suitable solvent to reduce the viscosity of the demulsif ⁇ er blend. Accordingly, there is an ongoing need for new, economical and effective chemicals and processes for resolving emulsions into the component parts of water and oil or brine, including processes and compositions that are suitable for cold climates.
- AFRA alkylphenol formaldehyde resin alkoxylates
- PAG polyalkylene glycols
- organic sulfonates and the like.
- Organic acids are commonly used in demulsif ⁇ er formulations to enhance performance.
- Organic acids (and occasionally inorganic acids) are also sometimes used as separate or supplementary treatments to conventional demulsifier formulations.
- Such acids or formulations containing acids require solvents to stabilize the blend, especially in cold climate conditions where freezing is an issue and pour points of less than -40 0 C are required.
- Inactive solvents comprise large proportions of the total volume of a demulsif ⁇ er blend, especially when the blend is used in cold climates. The purpose of such solvent is primarily viscosity reduction to allow handling and prevent freezing. The problem is that such blends contain significant amounts of solvent.
- a main challenge in oilfield production is the resolution of crude oil emulsions.
- the emulsions may be water-in-oil, oil-in-water, or complex or multiple emulsions (e.g., water- in-oil-in-water).
- a reverse emulsion breaker is typically used to treat water external emulsions and a standard emulsion breaker is normally used to treat oil external emulsions.
- Many reverse emulsion breakers also have a small window of treatment dosages, which makes it challenging and difficult to properly control resolution.
- Complex or multiple emulsions typically require both a reverse and a standard emulsion breaker to aid in its resolution into clean water and dry oil.
- demulsifier that is able to resolve complex or multiple emulsions in a single product application without the need for a two product resolution process. It is also desired to have a demulsifier composition capable of resolving water external and complex emulsions while having a broad dosage range.
- the present invention includes the use of anhydride compositions, including, for example, alkyl and aryl anhydrides, for use as a demulsifier in resolving emulsions of water and oil.
- the anhydride composition can be used alone or in a blend with other demulsifiers.
- Specific anhydrides suitable for use in the present invention include acetic and propionic, with the preferred anhydride being acetic anhydride.
- the anhydride composition can be added directly to crude oil or other compositions to be resolved.
- the demulsifier composition includes one or more anhydrides or in combination with other demulsifiers.
- the anhydride(s) may be used in an amount ranging between trace (which is around 0.5% or less by weight) and 100% by weight of the demulsifier composition.
- This invention further relates to a demulsifier composition formed from a blend of demulsifier and the anhydride.
- the demulsifier includes ionic and non-ionic surfactants.
- Specific demulsifiers for use in the composition include alkylphenol resin, alkoxylates and derivatives, polyglycol ethers and derivatives, amine alkoxylates and derivatives, polyamine alkoxylates and derivates, and combinations thereof.
- the demulsifier composition includes acetic anhydride in an amount ranging between about 1 % and about 99% by weight of the composition. More preferably, the acetic anhydride is added in an amount ranging between about 20% and about 80% by weight of the demulsifier composition.
- the acetic anhydride is added in an amount ranging between about 30% and about 60% by weight of the demulsifier composition.
- the anhydride can be used alone, so that the ultimate demulsifier composition contains an amount of the anhydride equal to between a trace amount and up to 100% by weight of the demulsifier composition.
- the invention also includes the use of one or more anhydrides as a solvent. Also, the invention includes using the anhydride(s) blended alone or with a demulsifier to form a demulsifier composition in which the anhydride functions as a solvent. As such, any amount of anhydride can be used as a solvent.
- the invention further includes a method of forming a demulsifier composition. This includes adding at ambient conditions an amount of anhydride to a known demulsifier.
- the invention includes a method for dehydrating crude oil, whereby an amount of the demulsifier composition is added to the crude oil.
- the demulsifier composition includes an anhydride, such as acetic anhydride, and potentially other constituents.
- the resultant demulsifier composition remains fluid at sub-zero temperatures including down to
- the anhydride may be used alone, where the demulsifier composition includes an amount of anhydride from trace to 100 wt%.
- An aspect of the invention includes a method for resolving water external (including multiple) emulsions of water and oil whereby an effective amount of a demulsifier composition is added to the emulsion.
- the invention also includes a method of resolving multiple emulsions in a single step demulsification process.
- the demulsifier composition is a reverse emulsion breaker. In another embodiment, the demulsifier composition is a combination reverse emulsion breaker and standard emulsion breaker.
- An advantage of the invention is to provide an emulsion breaker capable of resolving complex or multiple emulsions with a single product.
- Another advantage of the invention is to provide an emulsion breaker composition that is winterized for use in extreme cold conditions.
- a further advantage of the invention is to provide an emulsion breaker that does not demonstrate reduced resolving activity with overtreatment.
- the terra "demulsifier” as used herein refers to a class of chemicals used to aid the separation of emulsions (including water in oil, oil in water, and multiple emulsions). They are commonly used in the processing of crude oil, which is typically produced along with significant quantities of saline water. This water (and salt) must be removed from the crude oil prior to refining, otherwise significant corrosion problems can occur in the refining process. Demulsifiers are typically based on the following chemistry: acid catalysed phenol-formaldehyde resins, base catalysed phenol-formaldehyde resins,, polyamines, di-epoxides, polyols.
- demulsifier formulations are typically a mixture of two to four different chemistries in a carrier solvent(s), such as xylene, HAN, IPA, MeOH.
- acetic anhydride refers to acetyl oxide or acetic oxide of the formula (CH 3 CO) 2 O.
- the acetic anhydride is a colorless, mobile, strongly refractive liquid. It is miscible with alcohol, ether, and acetic acid; and decomposes in water to form acetic acid.
- the present invention relates to a demulsifier composition that includes anhydride and can include an amount of a known demulsifier.
- Suitable anhydrides include alkyl and aryl anhydrides, acetic anhydride being preferred.
- the resultant composition not only functions . as a demulsifier, but is also a stable fluid at low temperatures.
- the demulsifier composition functions in cold weather environments of -40 0 C and below and reduces the need for inactive solvents.
- the anhydride demulsifier composition of the present invention is effective for resolving a broad range of hydrocarbon emulsions encountered in crude oil production, refining, and chemical processing.
- Typical hydrocarbons include crude oil, refined oil, bitumen, condensate, slop oil, distillates, fuels, brines, and mixtures thereof.
- the demulsifiers are also useful for resolving emulsions in butadiene, styrene, acrylic acid, and other hydrocarbon monomer process streams.
- the anhydride offers demulsification performance similar to acids (organic or inorganic) but has an appreciable solubility for conventional demulsifier active ingredients.
- acetic anhydride has a freezing point of -73 0 C, making it versatile not only as an active ingredient but also as a winterizing solvent.
- the acetic anhydride demulsifiers can be used to demulsify water-in-oil emulsions in various production and refinery processes. In a refinery desalting process, the incoming crude is deliberately mixed with wash water to remove dissolved salts and other contaminants.
- the emulsion is admixed with an effective amount of the acetic anhydride demulsifiers.
- the demulsifier compositions are brought into contact with or caused to act upon the emulsion to be treated in any of the various methods now generally used in the petroleum industry to resolve or break crude petroleum oil emulsions with a chemical agent.
- the demulsifier composition comprises at least an anhydride and can also be a blend of at least a "demulsifying amount" of a demulsifier and anhydride, generally acetic anhydride.
- Demulsifiers such as ionic or non-ionic surfactants, may be used alone or in combination with any of a number of demulsifiers known in the art including fatty acids, fatly amines, glycols, and alkylphenol formaldehyde condensation products.
- Typical demulsifiers for breaking crude oil emulsions that may have utility in the compositions herein are described in U.S. Pat. Nos.
- Suitable "surfactants” are defined herein to include, but are not necessarily limited to alkylphenol resin such as, oxyalkylated alkyl phenol resins, oxyalkylated amines, glycol resin esters, polyglycol ethers and derivatives, such as bisphenol glycol ethers, bisphenol glycol esters, salts of alkylaryl sulfonic acid, decarbamates, oxyalkylated polyols reacted with compounds selected from the group consisting of diepoxides and polycarboxylic acids, unreacted oxyalkylated polyols, unreacted oxyalkylated phenolic resins, alkoxylates and derivatives, amine alkoxylates and derivatives, polyamine alkoxylates and derivatives, and combinations thereof.
- alkylphenol resin such as, oxyalkylated alkyl phenol resins, oxyalkylated amines, glycol resin esters, polyglycol ethers and derivatives
- the derivatives include post-reacted materials such as polyglycol ether which is often reacted with another polyglycol ether using a linking chemical.
- the polyglycol ether may be reacted with a resin, or any of these compositions may be slightly reacted with, for example, a fatty acid.
- the particular demulsifier or solubilizing surfactant used, as well as whether a single demulsfier or a combination of demulsifiers is used, will depend upon the emulsion properties of the produced fluids.
- the demulsifiers can be added in a variety of amounts including between broadly trace to about 100% or about 1% to about 99% by weight of the composition or between about 10% and about 90% by weight of the composition. More specifically, the demulsifier can be added in an amount equal to between about 20% and about 80% by weight of the composition or, about 40% and about 70% by weight of the demulsifier composition. More preferably, the demulsifier is added in an amount equal to between about 25% and about 50% by weight of the demulsifier composition.
- the anhydride demulsifier composition (“demulsifier composition”) is formed from an amount of anhydride and optionally a known demulsifier, such as the ones mentioned above.
- the anhydrides include alkyl and aryl anhydrides, specifically propionic and acetic anhydrides, with acetic anhydride being preferred.
- the anhydride blended with the demulsifier is typically neat, or nearly 100% pure. It can be added in any amount sufficient to produce a demulsification and winterizing solvent.
- the amount of anhydride mixed with the demulsifier can vary according to a particular use; however, it is generally added in an amount sufficient to prevent freezing of the demulsifier and allow for use in cold climates.
- the anhydride, and especially the acetic anhydride can be added in an amount equal to between trace and up to 100% by weight of the demulsifier composition. If the acetic anhydride is to be used as a principle solvent then it will preferably be added in an amount equal to between about 20% and about 80% by total weight of the demulsifier composition. More preferably the acetic anhydride is added in an amount equal to between about 30% and about 60% by weight of the demulsifier composition. The acetic anhydride can also be added in an amount equal to between about 50% and about 75% by weight of the demulsifier.
- the demulsifier composition can include an amount of anhydride, including acetic anhydride, ranging between trace or about 1% and up to about 99% or 100% by weight of the demulsifier composition.
- the demulsifier composition may also include corrosion inhibitors, viscosity reducers and other chemical treatments used in crude oil production, refining and chemical processing. Additional optional solvents could be added such as: xylene, toluene, light or heavy aromatic naphtha, and the like. Each component contributes to different treating characteristics when added to the crude oil emulsion due to their unique chemical properties.
- the acetic anhydride alone or with a demulsifier is blended together to form a chemical treatment suitable for application to the emulsion.
- the amount of the demulsifier composition used depends on the particular crude oil emulsion being treated. Although the amount added is typically at least 10 ppm. In general, the effective amount of demulsifier composition ranges from between about 10 ppm to about 1,000 ppm based on the volume of oil.
- the demulsif ⁇ er composition can be introduced into the crude oil emulsion by injecting beneath the surface into the oil well itself by injecting into the crude oil at the well-head or by injecting into the crude oil process stream at a point between and including the well-head and the final oil storage tank.
- the demulsifier composition may be injected continuously or in batch fashion. The injection step is preferably accomplished using electric or gas pumps.
- the treated crude oil emulsion is then allowed to separate into distinct layers of water and oil. Once separation into distinct layers of water and oil has been effected, various means known in the art can be utilized for withdrawing the free water and separating crude oil.
- a reservoir is provided to hold the composition of the invention in either diluted or undiluted form adjacent to the point where the effluent crude petroleum oil leaves the well.
- the reservoir is connected to a proportioning pump capable of dropwise injecting the demulsifier of the invention into the fluids leaving the well, which then pass through a flow line into a settling tank.
- the well fluids pass into the settling tank at the bottom of the tank so that incoming fluids do not disturb stratification of the layers of crude petroleum water and oil that takes place during the course of demulsification.
- the role of the demulsifier is usually to generate dry oil for use in downstream applications.
- SAGD steam-assisted gravity drainage
- the demulsifier is used to generate clean water. It should be appreciated that the invention has equal application in such SAGD processes, further explained in the examples below.
- Table 1 Listed in Table 1 below are a variety of compositions that were tested as demulsifiers. The testing was performed as a typical bottle test where 100 ml of warmed oil emulsion was contacted for a period of time with a demulsifier. The oil contained water in an amount equal to 15% by volume of the total mixture. The emulsions were heated to about 80 0 C. The demulsifiers were added as listed below in an amount ranging between about 300 ppm to about 2,400 ppm. The emulsion and demulsifier mix was shaken. Table 1
- Performance of the chemical treatment was evaluated by means of monitoring the volume of water that phase separated in the bottle over time (15 minutes, 25 minutes, 1 hour, and 2 hours) and also by determining the amount of residual water (percentage by volume) that remained in the oil at the end of the 2 hour period (far right column).
- D-87 and D-88 were designed to treat a a particular oilfield emulsion.
- the demulsifier and acid blends were both required to dehydrate the crude oil. Neither is capable of treatment on its own and treatment rates of both are high.
- D-88 is a conventional demulsifier blend comprising about 40% active ingredients (polymeric alkoxylates and derivatives) and about 60% inactive solvent (alcohol and aromatic hydrocarbon).
- D-87 is a 50% active solution of acetic acid in xylene and isopropyl alcohol. These solvents are required to prevent the acetic acid from freezing (it has a melting point of 16°C).
- Blend 215.1 is a novel blend comprising demulsifier active ingredients from D- 88 (25%) and acetic anhydride (75%). The laboratory test data shows that at 300 ppm this single blend performs equivalently to 1200 ppm D-88 plus 1200 ppm D-87. Moreover, blend 215.1 remains fluid and stable at temperatures of less than 40 0 C below zero, eliminating the need for inert solvents.
- Example 2
- a multiple (i.e., complex) emulsion taken from a SAGD facility was treated with acetic anhydride in a typical laboratory bottle test.
- the acetic anhydride liberated the water external phase as clean water at treat rates of 700 ppm (by volume) and above with little indication of overtreatment when used in excess (Table 2A).
- the dosages in Table 2 A are higher than typically used in a production facility and are used to demonstrate resistance to overtreatment.
- a traditional emulsion breaker (labeled REB in Table 2B) showed significantly reduced resolving ability above 200 ppm.
- the blend included a mixture of demulsifier ingredients in a solution of acetic anhydride. These ingredients were known to be effective in the dehydration of such types of crude oil and were fully soluble in the acetic anhydride solution. They comprised polymeric alkoxylates and derivatives including alklyphenol formaldehyde resins.
- Acetic anhydride is used as a dermilsifier. Tests are performed whereby a typical bottle test of 100 ml of warmed oil emulsion is contacted for a period of time with the acetic anhydride demulsif ⁇ er. The oil contains water in an amount equal to 15% by volume of the total mixture. The emulsions are heated to 80 0 C. The acetic anhydride is then added in an amount ranging between 300 ppm and 2400 ppm. The emulsion and demulsii ⁇ er mix is shaken.
- Performance of the chemical treatment is evaluated by means of monitoring the volume of water that phase separates in the bottle over time (15 minutes, 25 minutes, 1 hour, and
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Colloid Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US12/209,845 US9096805B2 (en) | 2008-06-04 | 2008-09-12 | Anhydride demulsifier formulations for resolving emulsions of water and oil |
PCT/US2009/056644 WO2010030867A1 (en) | 2008-09-12 | 2009-09-11 | Anhydride demulsifier formulations for resolving emulsions of water and oil |
Publications (2)
Publication Number | Publication Date |
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EP2370547A1 true EP2370547A1 (en) | 2011-10-05 |
EP2370547B1 EP2370547B1 (en) | 2017-10-25 |
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Application Number | Title | Priority Date | Filing Date |
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EP09792457.5A Not-in-force EP2370547B1 (en) | 2008-09-12 | 2009-09-11 | Use of an anhydride demulsifier formulation for resolving a water external emulsion of water and oil or a complex emulsion of water and oil and a method for resolving a water external emulsion of water and oil or a complex emulsion of water and oil using an anhydride demulsifier formulation |
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US (1) | US9096805B2 (en) |
EP (1) | EP2370547B1 (en) |
BR (1) | BRPI0918783B1 (en) |
CA (1) | CA2736367C (en) |
CO (1) | CO6351806A2 (en) |
GB (1) | GB2476022A (en) |
MX (1) | MX2011002633A (en) |
WO (1) | WO2010030867A1 (en) |
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US8969262B2 (en) * | 2008-06-04 | 2015-03-03 | Nalco Company | Utilization of an anhydride as a demulsifier and a solvent for demulsifier formulations |
US9096805B2 (en) * | 2008-06-04 | 2015-08-04 | Nalco Company | Anhydride demulsifier formulations for resolving emulsions of water and oil |
MX340805B (en) | 2011-04-18 | 2016-06-24 | Inst Mexicano Del Petróleo | Synergistic formulations of functionalized copolymers and ionic liquids for dehydrated and desalted of median, heavy and extra heavy crude oils. |
MX2013002243A (en) | 2013-02-26 | 2014-09-03 | Inst Mexicano Del Petróleo | Block copolymers, synthesis and application as dehydrating and desalting of heavy crudes. |
MX2013002359A (en) | 2013-02-28 | 2014-09-03 | Inst Mexicano Del Petróleo | Dehydrating and desalting compositions of crude oils, using triblock copolymers alpha,omega-bifunctionalized with amines. |
US9663726B2 (en) * | 2014-02-10 | 2017-05-30 | Baker Hughes Incorporated | Fluid compositions and methods for using cross-linked phenolic resins |
CN104531206B (en) * | 2014-12-05 | 2016-01-20 | 成都华阳兴华化工有限公司 | Environmental-protecting and high-efficient type low temperature condensate oil emulsion splitter and preparation method thereof |
CA2978437C (en) * | 2015-03-04 | 2023-09-19 | Ecolab Usa Inc. | Reverse emulsion breaker polymers from poly(triethanolamine) |
US9914882B2 (en) * | 2015-03-06 | 2018-03-13 | Ecolab Usa Inc. | Reverse emulsion breaker polymers |
US10414988B2 (en) | 2015-12-02 | 2019-09-17 | Ecolab Usa Inc. | Methods of treating a stream comprising crude oil and water |
EP3205701A1 (en) | 2016-02-11 | 2017-08-16 | Bp Oil International Limited | Fuel compositions |
EP3205704A1 (en) * | 2016-02-11 | 2017-08-16 | Bp Oil International Limited | Methods for demulsifying |
US11548784B1 (en) | 2021-10-26 | 2023-01-10 | Saudi Arabian Oil Company | Treating sulfur dioxide containing stream by acid aqueous absorption |
US12116326B2 (en) | 2021-11-22 | 2024-10-15 | Saudi Arabian Oil Company | Conversion of hydrogen sulfide and carbon dioxide into hydrocarbons using non-thermal plasma and a catalyst |
US12179129B2 (en) | 2021-12-14 | 2024-12-31 | Saudi Arabian Oil Company | Synergetic solvent for crude oil emulsion breakers |
US11926799B2 (en) | 2021-12-14 | 2024-03-12 | Saudi Arabian Oil Company | 2-iso-alkyl-2-(4-hydroxyphenyl)propane derivatives used as emulsion breakers for crude oil |
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2008
- 2008-09-12 US US12/209,845 patent/US9096805B2/en active Active
-
2009
- 2009-09-11 WO PCT/US2009/056644 patent/WO2010030867A1/en active Application Filing
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- 2009-09-11 CA CA2736367A patent/CA2736367C/en not_active Expired - Fee Related
- 2009-09-11 EP EP09792457.5A patent/EP2370547B1/en not_active Not-in-force
- 2009-09-11 BR BRPI0918783A patent/BRPI0918783B1/en not_active IP Right Cessation
- 2009-09-11 GB GB1105806A patent/GB2476022A/en not_active Withdrawn
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2011
- 2011-03-17 CO CO11033378A patent/CO6351806A2/en active IP Right Grant
Non-Patent Citations (1)
Title |
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See references of WO2010030867A1 * |
Also Published As
Publication number | Publication date |
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GB2476022A (en) | 2011-06-08 |
US20090306232A1 (en) | 2009-12-10 |
WO2010030867A1 (en) | 2010-03-18 |
BRPI0918783B1 (en) | 2018-08-28 |
GB201105806D0 (en) | 2011-05-18 |
CA2736367C (en) | 2016-10-25 |
BRPI0918783A2 (en) | 2015-12-01 |
EP2370547B1 (en) | 2017-10-25 |
MX2011002633A (en) | 2011-04-07 |
CO6351806A2 (en) | 2011-12-20 |
CA2736367A1 (en) | 2010-03-18 |
US9096805B2 (en) | 2015-08-04 |
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